Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP306907.RAl2RyiGSiNqGvXBvLUpiIehIIqRZ3KxDYMIzWktq8OGI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP306907.RAl2RyiGSiNqGvXBvLUpiIehIIqRZ3KxDYMIzWktq8OGI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP306907.RAl2RyiGSiNqGvXBvLUpiIehIIqRZ3KxDYMIzWktq8OGI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP306907.RAl2RyiGSiNqGvXBvLUpiIehIIqRZ3KxDYMIzWktq8OGI130_provenance.
- befree-20150227 importedOn "2015-02-27" NP306907.RAl2RyiGSiNqGvXBvLUpiIehIIqRZ3KxDYMIzWktq8OGI130_provenance.
- NP306907.RAl2RyiGSiNqGvXBvLUpiIehIIqRZ3KxDYMIzWktq8OGI130_assertion wasGeneratedBy ECO_0000203 NP306907.RAl2RyiGSiNqGvXBvLUpiIehIIqRZ3KxDYMIzWktq8OGI130_provenance.
- NP306907.RAl2RyiGSiNqGvXBvLUpiIehIIqRZ3KxDYMIzWktq8OGI130_assertion wasDerivedFrom befree-20150227 NP306907.RAl2RyiGSiNqGvXBvLUpiIehIIqRZ3KxDYMIzWktq8OGI130_provenance.
- NP306907.RAl2RyiGSiNqGvXBvLUpiIehIIqRZ3KxDYMIzWktq8OGI130_assertion SIO_000772 18674702 NP306907.RAl2RyiGSiNqGvXBvLUpiIehIIqRZ3KxDYMIzWktq8OGI130_provenance.
- NP306907.RAl2RyiGSiNqGvXBvLUpiIehIIqRZ3KxDYMIzWktq8OGI130_assertion evidence source_evidence_literature NP306907.RAl2RyiGSiNqGvXBvLUpiIehIIqRZ3KxDYMIzWktq8OGI130_provenance.
- NP306907.RAl2RyiGSiNqGvXBvLUpiIehIIqRZ3KxDYMIzWktq8OGI130_assertion description "[It is currently reserved for individuals with an increased risk for pancreatic ductal adenocarcinoma, such as those who have inherited genetic syndromes (eg, patients who have Peutz-Jeghers syndrome or hereditary pancreatitis, germline mutation carriers of p16 and BRCA2) and at-risk relatives of patients who have familial pancreatic cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP306907.RAl2RyiGSiNqGvXBvLUpiIehIIqRZ3KxDYMIzWktq8OGI130_provenance.