Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP451935.RA3EYfHO3EVuPQ2J0gLwrEAHL2StJw0S7bUfoS8N7Ss9w130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP451935.RA3EYfHO3EVuPQ2J0gLwrEAHL2StJw0S7bUfoS8N7Ss9w130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP451935.RA3EYfHO3EVuPQ2J0gLwrEAHL2StJw0S7bUfoS8N7Ss9w130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP451935.RA3EYfHO3EVuPQ2J0gLwrEAHL2StJw0S7bUfoS8N7Ss9w130_provenance.
- NP451935.RA3EYfHO3EVuPQ2J0gLwrEAHL2StJw0S7bUfoS8N7Ss9w130_assertion description "[De novo and inherited mutations in COL4A2, encoding the type IV collagen ?2 chain cause porencephaly.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP451935.RA3EYfHO3EVuPQ2J0gLwrEAHL2StJw0S7bUfoS8N7Ss9w130_provenance.
- NP451935.RA3EYfHO3EVuPQ2J0gLwrEAHL2StJw0S7bUfoS8N7Ss9w130_assertion evidence source_evidence_literature NP451935.RA3EYfHO3EVuPQ2J0gLwrEAHL2StJw0S7bUfoS8N7Ss9w130_provenance.
- NP451935.RA3EYfHO3EVuPQ2J0gLwrEAHL2StJw0S7bUfoS8N7Ss9w130_assertion SIO_000772 22209246 NP451935.RA3EYfHO3EVuPQ2J0gLwrEAHL2StJw0S7bUfoS8N7Ss9w130_provenance.
- NP451935.RA3EYfHO3EVuPQ2J0gLwrEAHL2StJw0S7bUfoS8N7Ss9w130_assertion wasDerivedFrom befree-20140225 NP451935.RA3EYfHO3EVuPQ2J0gLwrEAHL2StJw0S7bUfoS8N7Ss9w130_provenance.
- NP451935.RA3EYfHO3EVuPQ2J0gLwrEAHL2StJw0S7bUfoS8N7Ss9w130_assertion wasGeneratedBy ECO_0000203 NP451935.RA3EYfHO3EVuPQ2J0gLwrEAHL2StJw0S7bUfoS8N7Ss9w130_provenance.
- befree-20140225 importedOn "2014-02-25" NP451935.RA3EYfHO3EVuPQ2J0gLwrEAHL2StJw0S7bUfoS8N7Ss9w130_provenance.