Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP498723.RAXWy1liVd6UBqUYD-QRikYz3Rwd9Qc6hFkKkOJE-VWNU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP498723.RAXWy1liVd6UBqUYD-QRikYz3Rwd9Qc6hFkKkOJE-VWNU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP498723.RAXWy1liVd6UBqUYD-QRikYz3Rwd9Qc6hFkKkOJE-VWNU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP498723.RAXWy1liVd6UBqUYD-QRikYz3Rwd9Qc6hFkKkOJE-VWNU130_provenance.
- NP498723.RAXWy1liVd6UBqUYD-QRikYz3Rwd9Qc6hFkKkOJE-VWNU130_assertion description "[The other two patients are members of a large multigenerational family affected with familial MTC due to a germline mutation of the RET gene (Ala891Ser).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP498723.RAXWy1liVd6UBqUYD-QRikYz3Rwd9Qc6hFkKkOJE-VWNU130_provenance.
- NP498723.RAXWy1liVd6UBqUYD-QRikYz3Rwd9Qc6hFkKkOJE-VWNU130_assertion evidence source_evidence_literature NP498723.RAXWy1liVd6UBqUYD-QRikYz3Rwd9Qc6hFkKkOJE-VWNU130_provenance.
- NP498723.RAXWy1liVd6UBqUYD-QRikYz3Rwd9Qc6hFkKkOJE-VWNU130_assertion SIO_000772 15947103 NP498723.RAXWy1liVd6UBqUYD-QRikYz3Rwd9Qc6hFkKkOJE-VWNU130_provenance.
- NP498723.RAXWy1liVd6UBqUYD-QRikYz3Rwd9Qc6hFkKkOJE-VWNU130_assertion wasDerivedFrom befree-2016 NP498723.RAXWy1liVd6UBqUYD-QRikYz3Rwd9Qc6hFkKkOJE-VWNU130_provenance.
- NP498723.RAXWy1liVd6UBqUYD-QRikYz3Rwd9Qc6hFkKkOJE-VWNU130_assertion wasGeneratedBy ECO_0000203 NP498723.RAXWy1liVd6UBqUYD-QRikYz3Rwd9Qc6hFkKkOJE-VWNU130_provenance.
- befree-2016 importedOn "2016-02-19" NP498723.RAXWy1liVd6UBqUYD-QRikYz3Rwd9Qc6hFkKkOJE-VWNU130_provenance.