Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP217000.RAWaGcpvr-ENtvAj5rd4rnN9XSwKBNOQBWt7cD28dFnqw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP217000.RAWaGcpvr-ENtvAj5rd4rnN9XSwKBNOQBWt7cD28dFnqw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP217000.RAWaGcpvr-ENtvAj5rd4rnN9XSwKBNOQBWt7cD28dFnqw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP217000.RAWaGcpvr-ENtvAj5rd4rnN9XSwKBNOQBWt7cD28dFnqw130_provenance.
- NP217000.RAWaGcpvr-ENtvAj5rd4rnN9XSwKBNOQBWt7cD28dFnqw130_assertion description "[Mutations of the human androgen receptor gene were identified in five subjects from four families with androgen insensitivity syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP217000.RAWaGcpvr-ENtvAj5rd4rnN9XSwKBNOQBWt7cD28dFnqw130_provenance.
- NP217000.RAWaGcpvr-ENtvAj5rd4rnN9XSwKBNOQBWt7cD28dFnqw130_assertion evidence source_evidence_literature NP217000.RAWaGcpvr-ENtvAj5rd4rnN9XSwKBNOQBWt7cD28dFnqw130_provenance.
- NP217000.RAWaGcpvr-ENtvAj5rd4rnN9XSwKBNOQBWt7cD28dFnqw130_assertion SIO_000772 7581399 NP217000.RAWaGcpvr-ENtvAj5rd4rnN9XSwKBNOQBWt7cD28dFnqw130_provenance.
- NP217000.RAWaGcpvr-ENtvAj5rd4rnN9XSwKBNOQBWt7cD28dFnqw130_assertion wasDerivedFrom befree-20140225 NP217000.RAWaGcpvr-ENtvAj5rd4rnN9XSwKBNOQBWt7cD28dFnqw130_provenance.
- NP217000.RAWaGcpvr-ENtvAj5rd4rnN9XSwKBNOQBWt7cD28dFnqw130_assertion wasGeneratedBy ECO_0000203 NP217000.RAWaGcpvr-ENtvAj5rd4rnN9XSwKBNOQBWt7cD28dFnqw130_provenance.
- befree-20140225 importedOn "2014-02-25" NP217000.RAWaGcpvr-ENtvAj5rd4rnN9XSwKBNOQBWt7cD28dFnqw130_provenance.