Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP189521.RAPoRb9O0_hmFORA9BIAs0h6l_SURr98vi1RP6GkM2UwI130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP189521.RAPoRb9O0_hmFORA9BIAs0h6l_SURr98vi1RP6GkM2UwI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP189521.RAPoRb9O0_hmFORA9BIAs0h6l_SURr98vi1RP6GkM2UwI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP189521.RAPoRb9O0_hmFORA9BIAs0h6l_SURr98vi1RP6GkM2UwI130_provenance.
- NP189521.RAPoRb9O0_hmFORA9BIAs0h6l_SURr98vi1RP6GkM2UwI130_assertion description "[study performed in two samples of genetically homogeneous patients and controls does not support the suggestion that HFE mutations may be associated with acute myocardial infarction in susceptible individuals]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP189521.RAPoRb9O0_hmFORA9BIAs0h6l_SURr98vi1RP6GkM2UwI130_provenance.
- NP189521.RAPoRb9O0_hmFORA9BIAs0h6l_SURr98vi1RP6GkM2UwI130_assertion evidence source_evidence_literature NP189521.RAPoRb9O0_hmFORA9BIAs0h6l_SURr98vi1RP6GkM2UwI130_provenance.
- NP189521.RAPoRb9O0_hmFORA9BIAs0h6l_SURr98vi1RP6GkM2UwI130_assertion SIO_000772 12850485 NP189521.RAPoRb9O0_hmFORA9BIAs0h6l_SURr98vi1RP6GkM2UwI130_provenance.
- NP189521.RAPoRb9O0_hmFORA9BIAs0h6l_SURr98vi1RP6GkM2UwI130_assertion wasDerivedFrom lhgdn-20090331 NP189521.RAPoRb9O0_hmFORA9BIAs0h6l_SURr98vi1RP6GkM2UwI130_provenance.
- NP189521.RAPoRb9O0_hmFORA9BIAs0h6l_SURr98vi1RP6GkM2UwI130_assertion wasGeneratedBy ECO_0000203 NP189521.RAPoRb9O0_hmFORA9BIAs0h6l_SURr98vi1RP6GkM2UwI130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP189521.RAPoRb9O0_hmFORA9BIAs0h6l_SURr98vi1RP6GkM2UwI130_provenance.