Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP109246.RAq_VrpxDZ2X1eALWkaIAzYOakPAhP3-AbmFnUneF5ssE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP109246.RAq_VrpxDZ2X1eALWkaIAzYOakPAhP3-AbmFnUneF5ssE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP109246.RAq_VrpxDZ2X1eALWkaIAzYOakPAhP3-AbmFnUneF5ssE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP109246.RAq_VrpxDZ2X1eALWkaIAzYOakPAhP3-AbmFnUneF5ssE130_provenance.
- NP109246.RAq_VrpxDZ2X1eALWkaIAzYOakPAhP3-AbmFnUneF5ssE130_assertion description "[resequencing analysis does not support the existence of deleterious, gain-of-function or transcription mutations in HSD17B1, which could explain the clustering of breast cancer cases in non-BRCA1/2 high-risk French Canadian families ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP109246.RAq_VrpxDZ2X1eALWkaIAzYOakPAhP3-AbmFnUneF5ssE130_provenance.
- NP109246.RAq_VrpxDZ2X1eALWkaIAzYOakPAhP3-AbmFnUneF5ssE130_assertion evidence source_evidence_literature NP109246.RAq_VrpxDZ2X1eALWkaIAzYOakPAhP3-AbmFnUneF5ssE130_provenance.
- NP109246.RAq_VrpxDZ2X1eALWkaIAzYOakPAhP3-AbmFnUneF5ssE130_assertion SIO_000772 18083510 NP109246.RAq_VrpxDZ2X1eALWkaIAzYOakPAhP3-AbmFnUneF5ssE130_provenance.
- NP109246.RAq_VrpxDZ2X1eALWkaIAzYOakPAhP3-AbmFnUneF5ssE130_assertion wasDerivedFrom lhgdn-20090331 NP109246.RAq_VrpxDZ2X1eALWkaIAzYOakPAhP3-AbmFnUneF5ssE130_provenance.
- NP109246.RAq_VrpxDZ2X1eALWkaIAzYOakPAhP3-AbmFnUneF5ssE130_assertion wasGeneratedBy ECO_0000203 NP109246.RAq_VrpxDZ2X1eALWkaIAzYOakPAhP3-AbmFnUneF5ssE130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP109246.RAq_VrpxDZ2X1eALWkaIAzYOakPAhP3-AbmFnUneF5ssE130_provenance.