Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP925562.RAP__QfEERrNGCXXyZWDfbjFGt15F0IuzoyHAk4HA7Imw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP925562.RAP__QfEERrNGCXXyZWDfbjFGt15F0IuzoyHAk4HA7Imw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP925562.RAP__QfEERrNGCXXyZWDfbjFGt15F0IuzoyHAk4HA7Imw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP925562.RAP__QfEERrNGCXXyZWDfbjFGt15F0IuzoyHAk4HA7Imw130_provenance.
- NP925562.RAP__QfEERrNGCXXyZWDfbjFGt15F0IuzoyHAk4HA7Imw130_assertion description "[In a Portuguese population of 45 HCM patients, 5 (11.1%) had mutations in the MYBPC3 gene (3 missense mutations--theoretically less frequent in the MYBPC3 gene--and 2 deletions).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP925562.RAP__QfEERrNGCXXyZWDfbjFGt15F0IuzoyHAk4HA7Imw130_provenance.
- NP925562.RAP__QfEERrNGCXXyZWDfbjFGt15F0IuzoyHAk4HA7Imw130_assertion evidence source_evidence_literature NP925562.RAP__QfEERrNGCXXyZWDfbjFGt15F0IuzoyHAk4HA7Imw130_provenance.
- NP925562.RAP__QfEERrNGCXXyZWDfbjFGt15F0IuzoyHAk4HA7Imw130_assertion SIO_000772 16566405 NP925562.RAP__QfEERrNGCXXyZWDfbjFGt15F0IuzoyHAk4HA7Imw130_provenance.
- NP925562.RAP__QfEERrNGCXXyZWDfbjFGt15F0IuzoyHAk4HA7Imw130_assertion wasDerivedFrom befree-20150227 NP925562.RAP__QfEERrNGCXXyZWDfbjFGt15F0IuzoyHAk4HA7Imw130_provenance.
- NP925562.RAP__QfEERrNGCXXyZWDfbjFGt15F0IuzoyHAk4HA7Imw130_assertion wasGeneratedBy ECO_0000203 NP925562.RAP__QfEERrNGCXXyZWDfbjFGt15F0IuzoyHAk4HA7Imw130_provenance.
- befree-20150227 importedOn "2015-02-27" NP925562.RAP__QfEERrNGCXXyZWDfbjFGt15F0IuzoyHAk4HA7Imw130_provenance.