Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP19467.RA7IrnU-3wevrSyJ7KB-T7B6ExG81qxBlJusAB9obV_JU130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP19467.RA7IrnU-3wevrSyJ7KB-T7B6ExG81qxBlJusAB9obV_JU130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP19467.RA7IrnU-3wevrSyJ7KB-T7B6ExG81qxBlJusAB9obV_JU130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP19467.RA7IrnU-3wevrSyJ7KB-T7B6ExG81qxBlJusAB9obV_JU130_provenance.
- ctd_human-20150221 importedOn "2015-02-21" NP19467.RA7IrnU-3wevrSyJ7KB-T7B6ExG81qxBlJusAB9obV_JU130_provenance.
- NP19467.RA7IrnU-3wevrSyJ7KB-T7B6ExG81qxBlJusAB9obV_JU130_assertion wasGeneratedBy ECO_0000218 NP19467.RA7IrnU-3wevrSyJ7KB-T7B6ExG81qxBlJusAB9obV_JU130_provenance.
- NP19467.RA7IrnU-3wevrSyJ7KB-T7B6ExG81qxBlJusAB9obV_JU130_assertion wasDerivedFrom ctd_human-20150221 NP19467.RA7IrnU-3wevrSyJ7KB-T7B6ExG81qxBlJusAB9obV_JU130_provenance.
- NP19467.RA7IrnU-3wevrSyJ7KB-T7B6ExG81qxBlJusAB9obV_JU130_assertion SIO_000772 20023659 NP19467.RA7IrnU-3wevrSyJ7KB-T7B6ExG81qxBlJusAB9obV_JU130_provenance.
- NP19467.RA7IrnU-3wevrSyJ7KB-T7B6ExG81qxBlJusAB9obV_JU130_assertion evidence source_evidence_curated NP19467.RA7IrnU-3wevrSyJ7KB-T7B6ExG81qxBlJusAB9obV_JU130_provenance.
- NP19467.RA7IrnU-3wevrSyJ7KB-T7B6ExG81qxBlJusAB9obV_JU130_assertion description "[Mutations in the formin gene INF2 cause focal segmental glomerulosclerosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP19467.RA7IrnU-3wevrSyJ7KB-T7B6ExG81qxBlJusAB9obV_JU130_provenance.