Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP401173.RANJmwWq1ngup-XjK5levw_k5ojE_MCob5dahjKiXiO08130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP401173.RANJmwWq1ngup-XjK5levw_k5ojE_MCob5dahjKiXiO08130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP401173.RANJmwWq1ngup-XjK5levw_k5ojE_MCob5dahjKiXiO08130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP401173.RANJmwWq1ngup-XjK5levw_k5ojE_MCob5dahjKiXiO08130_provenance.
- NP401173.RANJmwWq1ngup-XjK5levw_k5ojE_MCob5dahjKiXiO08130_assertion description "[DNA samples from 50 individuals affected with breast cancer from non-BRCA1/2 French Canadian families with a high risk of breast and ovarian cancer were screened for sequence variants in HSD17B1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP401173.RANJmwWq1ngup-XjK5levw_k5ojE_MCob5dahjKiXiO08130_provenance.
- NP401173.RANJmwWq1ngup-XjK5levw_k5ojE_MCob5dahjKiXiO08130_assertion evidence source_evidence_literature NP401173.RANJmwWq1ngup-XjK5levw_k5ojE_MCob5dahjKiXiO08130_provenance.
- NP401173.RANJmwWq1ngup-XjK5levw_k5ojE_MCob5dahjKiXiO08130_assertion SIO_000772 18083510 NP401173.RANJmwWq1ngup-XjK5levw_k5ojE_MCob5dahjKiXiO08130_provenance.
- NP401173.RANJmwWq1ngup-XjK5levw_k5ojE_MCob5dahjKiXiO08130_assertion wasDerivedFrom befree-20140225 NP401173.RANJmwWq1ngup-XjK5levw_k5ojE_MCob5dahjKiXiO08130_provenance.
- NP401173.RANJmwWq1ngup-XjK5levw_k5ojE_MCob5dahjKiXiO08130_assertion wasGeneratedBy ECO_0000203 NP401173.RANJmwWq1ngup-XjK5levw_k5ojE_MCob5dahjKiXiO08130_provenance.
- befree-20140225 importedOn "2014-02-25" NP401173.RANJmwWq1ngup-XjK5levw_k5ojE_MCob5dahjKiXiO08130_provenance.