http://rdf.disgenet.org/resource/nanopub/NP903615.RArlW7zjVENTYZrCVaPKDHUAkQMygUSVMfdkUm89n59kc#head
http://rdf.disgenet.org/resource/nanopub/NP903615.RArlW7zjVENTYZrCVaPKDHUAkQMygUSVMfdkUm89n59kc
http://www.nanopub.org/nschema#hasAssertion
http://rdf.disgenet.org/resource/nanopub/NP903615.RArlW7zjVENTYZrCVaPKDHUAkQMygUSVMfdkUm89n59kc#assertion
http://rdf.disgenet.org/resource/nanopub/NP903615.RArlW7zjVENTYZrCVaPKDHUAkQMygUSVMfdkUm89n59kc
http://www.nanopub.org/nschema#hasProvenance
http://rdf.disgenet.org/resource/nanopub/NP903615.RArlW7zjVENTYZrCVaPKDHUAkQMygUSVMfdkUm89n59kc#provenance
http://rdf.disgenet.org/resource/nanopub/NP903615.RArlW7zjVENTYZrCVaPKDHUAkQMygUSVMfdkUm89n59kc
http://www.nanopub.org/nschema#hasPublicationInfo
http://rdf.disgenet.org/resource/nanopub/NP903615.RArlW7zjVENTYZrCVaPKDHUAkQMygUSVMfdkUm89n59kc#publicationInfo
http://rdf.disgenet.org/resource/nanopub/NP903615.RArlW7zjVENTYZrCVaPKDHUAkQMygUSVMfdkUm89n59kc
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://www.nanopub.org/nschema#Nanopublication
http://rdf.disgenet.org/resource/nanopub/NP903615.RArlW7zjVENTYZrCVaPKDHUAkQMygUSVMfdkUm89n59kc#assertion
http://rdf.disgenet.org/resource/gda/DGNf309457878b8480b7dbdf4dc17a45e26
http://semanticscience.org/resource/SIO_000628
http://identifiers.org/ncbigene/5979
http://rdf.disgenet.org/resource/gda/DGNf309457878b8480b7dbdf4dc17a45e26
http://semanticscience.org/resource/SIO_000628
http://linkedlifedata.com/resource/umls/id/C0019569
http://rdf.disgenet.org/resource/gda/DGNf309457878b8480b7dbdf4dc17a45e26
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://semanticscience.org/resource/SIO_001122
http://rdf.disgenet.org/resource/nanopub/NP903615.RArlW7zjVENTYZrCVaPKDHUAkQMygUSVMfdkUm89n59kc#provenance
http://rdf.disgenet.org/resource/nanopub/NP903615.RArlW7zjVENTYZrCVaPKDHUAkQMygUSVMfdkUm89n59kc#assertion
http://purl.org/dc/terms/description
[RET is a receptor tyrosine kinase gene which is responsible for three different inherited cancer syndromes namely multiple endocrine neoplasia type 2A (MEN 2A), type 2B (MEN 2B) and familial medullary thyroid carcinoma (FMTC) as well as for Hirschsprung disease (HSCR), a congenital disorder affecting the intestinal motility.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
http://rdf.disgenet.org/resource/nanopub/NP903615.RArlW7zjVENTYZrCVaPKDHUAkQMygUSVMfdkUm89n59kc#assertion
http://purl.org/ontology/wi/core#evidence
http://rdf.disgenet.org/v5.0.0/void/source_evidence_literature
http://rdf.disgenet.org/resource/nanopub/NP903615.RArlW7zjVENTYZrCVaPKDHUAkQMygUSVMfdkUm89n59kc#assertion
http://semanticscience.org/resource/SIO_000772
http://identifiers.org/pubmed/7784092
http://rdf.disgenet.org/resource/nanopub/NP903615.RArlW7zjVENTYZrCVaPKDHUAkQMygUSVMfdkUm89n59kc#assertion
http://www.w3.org/ns/prov#wasDerivedFrom
http://rdf.disgenet.org/v5.0.0/void/BEFREE
http://rdf.disgenet.org/resource/nanopub/NP903615.RArlW7zjVENTYZrCVaPKDHUAkQMygUSVMfdkUm89n59kc#assertion
http://www.w3.org/ns/prov#wasGeneratedBy
http://purl.obolibrary.org/obo/ECO_0000203
http://rdf.disgenet.org/v5.0.0/void/BEFREE
http://purl.org/pav/importedOn
2017-02-19
http://rdf.disgenet.org/v5.0.0/void/source_evidence_literature
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.obolibrary.org/obo/ECO_0000212
http://rdf.disgenet.org/v5.0.0/void/source_evidence_literature
http://www.w3.org/2000/01/rdf-schema#comment
Gene-disease associations inferred from text-mining the literature.
http://rdf.disgenet.org/v5.0.0/void/source_evidence_literature
http://www.w3.org/2000/01/rdf-schema#label
DisGeNET evidence - LITERATURE
http://rdf.disgenet.org/resource/nanopub/NP903615.RArlW7zjVENTYZrCVaPKDHUAkQMygUSVMfdkUm89n59kc#publicationInfo
http://rdf.disgenet.org/resource/nanopub/NP903615.RArlW7zjVENTYZrCVaPKDHUAkQMygUSVMfdkUm89n59kc
http://purl.org/dc/terms/created
2017-10-17T13:15:56+02:00
http://rdf.disgenet.org/resource/nanopub/NP903615.RArlW7zjVENTYZrCVaPKDHUAkQMygUSVMfdkUm89n59kc
http://purl.org/dc/terms/rights
http://opendatacommons.org/licenses/odbl/1.0/
http://rdf.disgenet.org/resource/nanopub/NP903615.RArlW7zjVENTYZrCVaPKDHUAkQMygUSVMfdkUm89n59kc
http://purl.org/dc/terms/rightsHolder
http://rdf.disgenet.org/v5.0.0/void/IBIGroup
http://rdf.disgenet.org/resource/nanopub/NP903615.RArlW7zjVENTYZrCVaPKDHUAkQMygUSVMfdkUm89n59kc
http://purl.org/dc/terms/subject
http://semanticscience.org/resource/SIO_000983
http://rdf.disgenet.org/resource/nanopub/NP903615.RArlW7zjVENTYZrCVaPKDHUAkQMygUSVMfdkUm89n59kc
http://purl.org/net/provenance/ns#usedData
http://rdf.disgenet.org/v5.0.0/void/disgenetv3.0rdf
http://rdf.disgenet.org/resource/nanopub/NP903615.RArlW7zjVENTYZrCVaPKDHUAkQMygUSVMfdkUm89n59kc
http://purl.org/pav/authoredBy
http://orcid.org/0000-0001-5999-6269
http://rdf.disgenet.org/resource/nanopub/NP903615.RArlW7zjVENTYZrCVaPKDHUAkQMygUSVMfdkUm89n59kc
http://purl.org/pav/authoredBy
http://orcid.org/0000-0002-7534-7661
http://rdf.disgenet.org/resource/nanopub/NP903615.RArlW7zjVENTYZrCVaPKDHUAkQMygUSVMfdkUm89n59kc
http://purl.org/pav/authoredBy
http://orcid.org/0000-0002-9383-528X
http://rdf.disgenet.org/resource/nanopub/NP903615.RArlW7zjVENTYZrCVaPKDHUAkQMygUSVMfdkUm89n59kc
http://purl.org/pav/authoredBy
http://orcid.org/0000-0003-0169-8159
http://rdf.disgenet.org/resource/nanopub/NP903615.RArlW7zjVENTYZrCVaPKDHUAkQMygUSVMfdkUm89n59kc
http://purl.org/pav/authoredBy
http://orcid.org/0000-0003-1244-7654
http://rdf.disgenet.org/resource/nanopub/NP903615.RArlW7zjVENTYZrCVaPKDHUAkQMygUSVMfdkUm89n59kc
http://purl.org/pav/createdBy
http://orcid.org/0000-0003-0169-8159
http://rdf.disgenet.org/resource/nanopub/NP903615.RArlW7zjVENTYZrCVaPKDHUAkQMygUSVMfdkUm89n59kc
http://purl.org/pav/version
v5.0.0.0
http://rdf.disgenet.org/v5.0.0/void/disgenetv3.0rdf
http://purl.org/pav/version
v5.0.0