Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP4041.RArsxpRYkUgm4Xhh-pTgJGIAVRKeJFtd05682_PzTnIrc130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_curated type ECO_0000205 NP4041.RArsxpRYkUgm4Xhh-pTgJGIAVRKeJFtd05682_PzTnIrc130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP4041.RArsxpRYkUgm4Xhh-pTgJGIAVRKeJFtd05682_PzTnIrc130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP4041.RArsxpRYkUgm4Xhh-pTgJGIAVRKeJFtd05682_PzTnIrc130_provenance.
- NP4041.RArsxpRYkUgm4Xhh-pTgJGIAVRKeJFtd05682_PzTnIrc130_assertion description "[New mutations in MID1 provide support for loss of function as the cause of X-linked Opitz syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP4041.RArsxpRYkUgm4Xhh-pTgJGIAVRKeJFtd05682_PzTnIrc130_provenance.
- NP4041.RArsxpRYkUgm4Xhh-pTgJGIAVRKeJFtd05682_PzTnIrc130_assertion evidence source_evidence_curated NP4041.RArsxpRYkUgm4Xhh-pTgJGIAVRKeJFtd05682_PzTnIrc130_provenance.
- NP4041.RArsxpRYkUgm4Xhh-pTgJGIAVRKeJFtd05682_PzTnIrc130_assertion SIO_000772 11030761 NP4041.RArsxpRYkUgm4Xhh-pTgJGIAVRKeJFtd05682_PzTnIrc130_provenance.
- NP4041.RArsxpRYkUgm4Xhh-pTgJGIAVRKeJFtd05682_PzTnIrc130_assertion wasDerivedFrom uniprot-20130724 NP4041.RArsxpRYkUgm4Xhh-pTgJGIAVRKeJFtd05682_PzTnIrc130_provenance.
- NP4041.RArsxpRYkUgm4Xhh-pTgJGIAVRKeJFtd05682_PzTnIrc130_assertion wasGeneratedBy ECO_0000218 NP4041.RArsxpRYkUgm4Xhh-pTgJGIAVRKeJFtd05682_PzTnIrc130_provenance.
- uniprot-20130724 importedOn "2013-07-24" NP4041.RArsxpRYkUgm4Xhh-pTgJGIAVRKeJFtd05682_PzTnIrc130_provenance.