Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1294561.RA7xpG_S__bVvjJPBn9GrqyUUuXFnxAo9sWKbd2Xn5S0s130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP1294561.RA7xpG_S__bVvjJPBn9GrqyUUuXFnxAo9sWKbd2Xn5S0s130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1294561.RA7xpG_S__bVvjJPBn9GrqyUUuXFnxAo9sWKbd2Xn5S0s130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1294561.RA7xpG_S__bVvjJPBn9GrqyUUuXFnxAo9sWKbd2Xn5S0s130_provenance.
- NP1294561.RA7xpG_S__bVvjJPBn9GrqyUUuXFnxAo9sWKbd2Xn5S0s130_assertion description "[The phenotypes of the platelet-specific TMEM16F-null mice resemble those of patients with Scott syndrome, a mild bleeding disorder, indicating that these mice may provide a useful model for human Scott syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1294561.RA7xpG_S__bVvjJPBn9GrqyUUuXFnxAo9sWKbd2Xn5S0s130_provenance.
- NP1294561.RA7xpG_S__bVvjJPBn9GrqyUUuXFnxAo9sWKbd2Xn5S0s130_assertion evidence source_evidence_literature NP1294561.RA7xpG_S__bVvjJPBn9GrqyUUuXFnxAo9sWKbd2Xn5S0s130_provenance.
- NP1294561.RA7xpG_S__bVvjJPBn9GrqyUUuXFnxAo9sWKbd2Xn5S0s130_assertion SIO_000772 26417084 NP1294561.RA7xpG_S__bVvjJPBn9GrqyUUuXFnxAo9sWKbd2Xn5S0s130_provenance.
- NP1294561.RA7xpG_S__bVvjJPBn9GrqyUUuXFnxAo9sWKbd2Xn5S0s130_assertion wasDerivedFrom befree-2016 NP1294561.RA7xpG_S__bVvjJPBn9GrqyUUuXFnxAo9sWKbd2Xn5S0s130_provenance.
- NP1294561.RA7xpG_S__bVvjJPBn9GrqyUUuXFnxAo9sWKbd2Xn5S0s130_assertion wasGeneratedBy ECO_0000203 NP1294561.RA7xpG_S__bVvjJPBn9GrqyUUuXFnxAo9sWKbd2Xn5S0s130_provenance.
- befree-2016 importedOn "2016-02-19" NP1294561.RA7xpG_S__bVvjJPBn9GrqyUUuXFnxAo9sWKbd2Xn5S0s130_provenance.