Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP904876.RAojORNhxQHXApjqs-nHUdSNfMVWs9r3p3RdWTmMH-b_k130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP904876.RAojORNhxQHXApjqs-nHUdSNfMVWs9r3p3RdWTmMH-b_k130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP904876.RAojORNhxQHXApjqs-nHUdSNfMVWs9r3p3RdWTmMH-b_k130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP904876.RAojORNhxQHXApjqs-nHUdSNfMVWs9r3p3RdWTmMH-b_k130_provenance.
- NP904876.RAojORNhxQHXApjqs-nHUdSNfMVWs9r3p3RdWTmMH-b_k130_assertion description "[Given the complexity of HDGC, not only with regard to the management of the DGC risk, but also with regard to the risk for other related cancers, such as LBC, a multi-disciplinary approach is needed for the management of individuals with known CDH1 mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP904876.RAojORNhxQHXApjqs-nHUdSNfMVWs9r3p3RdWTmMH-b_k130_provenance.
- NP904876.RAojORNhxQHXApjqs-nHUdSNfMVWs9r3p3RdWTmMH-b_k130_assertion evidence source_evidence_literature NP904876.RAojORNhxQHXApjqs-nHUdSNfMVWs9r3p3RdWTmMH-b_k130_provenance.
- NP904876.RAojORNhxQHXApjqs-nHUdSNfMVWs9r3p3RdWTmMH-b_k130_assertion SIO_000772 18046629 NP904876.RAojORNhxQHXApjqs-nHUdSNfMVWs9r3p3RdWTmMH-b_k130_provenance.
- NP904876.RAojORNhxQHXApjqs-nHUdSNfMVWs9r3p3RdWTmMH-b_k130_assertion wasDerivedFrom befree-20150227 NP904876.RAojORNhxQHXApjqs-nHUdSNfMVWs9r3p3RdWTmMH-b_k130_provenance.
- NP904876.RAojORNhxQHXApjqs-nHUdSNfMVWs9r3p3RdWTmMH-b_k130_assertion wasGeneratedBy ECO_0000203 NP904876.RAojORNhxQHXApjqs-nHUdSNfMVWs9r3p3RdWTmMH-b_k130_provenance.
- befree-20150227 importedOn "2015-02-27" NP904876.RAojORNhxQHXApjqs-nHUdSNfMVWs9r3p3RdWTmMH-b_k130_provenance.