Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1312018.RAXR8v0fyB1ur5te4Tl1vwiFWNIZZfaiBA7221ntGF7QA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1312018.RAXR8v0fyB1ur5te4Tl1vwiFWNIZZfaiBA7221ntGF7QA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1312018.RAXR8v0fyB1ur5te4Tl1vwiFWNIZZfaiBA7221ntGF7QA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1312018.RAXR8v0fyB1ur5te4Tl1vwiFWNIZZfaiBA7221ntGF7QA130_provenance.
- NP1312018.RAXR8v0fyB1ur5te4Tl1vwiFWNIZZfaiBA7221ntGF7QA130_assertion description "[It is important to determine the STS activity in the propositus mother of apparently non familial cases of XLI to identify the carrier state and provide and accurate genetic counseling, as most of these seem to correspond to inherited cases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1312018.RAXR8v0fyB1ur5te4Tl1vwiFWNIZZfaiBA7221ntGF7QA130_provenance.
- NP1312018.RAXR8v0fyB1ur5te4Tl1vwiFWNIZZfaiBA7221ntGF7QA130_assertion evidence source_evidence_literature NP1312018.RAXR8v0fyB1ur5te4Tl1vwiFWNIZZfaiBA7221ntGF7QA130_provenance.
- NP1312018.RAXR8v0fyB1ur5te4Tl1vwiFWNIZZfaiBA7221ntGF7QA130_assertion SIO_000772 7546451 NP1312018.RAXR8v0fyB1ur5te4Tl1vwiFWNIZZfaiBA7221ntGF7QA130_provenance.
- NP1312018.RAXR8v0fyB1ur5te4Tl1vwiFWNIZZfaiBA7221ntGF7QA130_assertion wasDerivedFrom befree-2016 NP1312018.RAXR8v0fyB1ur5te4Tl1vwiFWNIZZfaiBA7221ntGF7QA130_provenance.
- NP1312018.RAXR8v0fyB1ur5te4Tl1vwiFWNIZZfaiBA7221ntGF7QA130_assertion wasGeneratedBy ECO_0000203 NP1312018.RAXR8v0fyB1ur5te4Tl1vwiFWNIZZfaiBA7221ntGF7QA130_provenance.
- befree-2016 importedOn "2016-02-19" NP1312018.RAXR8v0fyB1ur5te4Tl1vwiFWNIZZfaiBA7221ntGF7QA130_provenance.